A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033892



Internal ID19123114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17734226..17757583hg38UCSC Ensembl
Innerchr9:17734224..17757581hg19UCSC Ensembl
Innerchr9:17724224..17747581hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3823358
hg1923358
hg1823358
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755825
Samples
Known GenesSH3GL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033892
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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